東北大学 · Materials Science
히로토모 이시하라 교수의 연구실은 나노구조 탄소 소재의 설계 및 응용에 중점을 두고 있으며, 주로 템플릿 탄소화법을 활용해 정밀하게 구조가 제어된 다공성 탄소 재료를 개발합니다. 특히 제올라이트를 템플릿으로 사용한 미세다공성 탄소(zeolite-templated carbon, ZTC)를 중심으로 수소 저장, 전기화학적 커패시터, 리튬이온 배터리 등 에너지 저장 응용 분야에서 뛰어난 성능을 확보하고 있습니다. 연구는 나노미세 구조 제어, 표면 특성 조절, 전기화학적 거동 이해에 이르기까지 다각도로 진행되고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
The template carbonization method is a powerful tool for producing carbon materials with precisely controlled structures at the nanometer level. The resulting templated nanocarbons exhibit extraordinarily unique (often ordered) structures that could never be produced by any of the conventional methods for carbon production. This review summarizes recent publications about templated nanocarbons and their composites used for energy storage applications, including hydrogen storage, electrochemical
Zeolite-templated carbons (ZTCs) are ordered microporous carbons synthesized by using zeolite as a sacrificial template. Unlike well-known ordered mesoporous carbons obtained by using mesoporous silica templates, ZTCs consist of curved and single-layer graphene frameworks, thereby affording uniform micropore size (ca. 1.2 nm), developed microporosity (∼1.7 cm3 g-1), very high surface area (∼4000 m2 g-1), good compatibility with chemical modification, and remarkable softness/elasticity. Thus, ZTC
Ordered macroporous silica, a silica gel microhoneycomb (SMH), has been prepared through a method which uses micrometer-sized ice crystals as a template. Template ice crystals, which have a continuous rod shape, a polygonal cross section, and ordered diameters, were grown inside precursor silica hydrogels under a condition where the pseudo-steady-state growth of them continues. Besides their ordered macroporosity, micro-/mesopores develop inside the honeycomb walls through the freeze-drying of S
Super-stable mesoporous carbon sheet made of edge-free graphene walls enabled the assembly of symmetric supercapacitors with excellent stability under 3.5 V@60 °C and 4.4 V@25 °C conditions, even with a conventional electrolyte.
High-pressure hydrogen storage in zeolite-templated carbon (ZTC) was investigated at room temperature (30 °C). Several types of ZTCs with different surface areas and a nitrogen-doped ZTC were prepared. Their hydrogen storage performance at room temperature was examined and the results were compared with those of commercial activated carbons. At pressures below 10 MPa, the hydrogen uptake capacity was simply proportional to specific surface areas of the carbons, and both ZTCs and activated carbon
An ordered microporous carbon, which was prepared with zeolite as a template, was used as a model material to understand the ion storage/transfer behavior in electrical double-layer capacitor (EDLC). Several types of such zeolite-templated carbons (ZTCs) with different structures (framework regularity, particle size and pore diameter) were prepared and their EDLC performances were evaluated in an organic electrolyte solution (1 M Et(4)NBF(4)/propylene carbonate). Moreover, a simple method to eva
An oxidation‐resistant and elastic mesoporous carbon, graphene mesosponge (GMS), is prepared. GMS has a sponge‐like mesoporous framework (mean pore size is 5.8 nm) consisting mostly of single‐layer graphene walls, which realizes a high electric conductivity and a large surface area (1940 m 2 g −1 ). Moreover, the graphene‐based framework includes only a very small amount of edge sites, thereby achieving much higher stability against oxidation than conventional porous carbons such as carbon black
Despite recent advances in the carbonization of organic crystalline solids like metal-organic frameworks or supramolecular frameworks, it has been challenging to convert crystalline organic solids into ordered carbonaceous frameworks. Herein, we report a route to attaining such ordered frameworks via the carbonization of an organic crystal of a Ni-containing cyclic porphyrin dimer (Ni<sub>2</sub>-CPD<sub>Py</sub>). This dimer comprises two Ni-porphyrins linked by two butadiyne (diacetylene) moie
MgO has specific catalysis for CH<sub>4</sub>-to-C conversion, and functions as a cost-effective and environmentally friendly template to produce graphene mesosponge with developed porosity, excellent stability, and super soft and elastic properties.